Home NDC 71335-2017-01 NDC 71335-2017-01 - Duloxetine This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 71335-2017
Requested NDC 71335-2017-01
Package NDCs from labels 71335-2017-1, 71335-2017-2, 71335-2017-3, 71335-2017-4, 71335-2017-5, 71335-2017-6, 71335-2017-7, 71335-2017-8, 71335-2017-01
Manufacturer Bryant Ranch Prepack
Effective date 2024-08-07
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Duloxetine - Bryant Ranch Prepack Bryant Ranch Prepack 2024-08-07 HUMAN PRESCRIPTION DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71335-2017-1 Duloxetine 30 in 1 BOTTLE CAPSULE, DELAYED RELEASE 30 103 71335-2017-2 Duloxetine 60 in 1 BOTTLE CAPSULE, DELAYED RELEASE 60 103 71335-2017-3 Duloxetine 28 in 1 BOTTLE CAPSULE, DELAYED RELEASE 28 103 71335-2017-4 Duloxetine 6 in 1 BOTTLE CAPSULE, DELAYED RELEASE 6 103 71335-2017-5 Duloxetine 90 in 1 BOTTLE CAPSULE, DELAYED RELEASE 90 103 71335-2017-6 Duloxetine 15 in 1 BOTTLE CAPSULE, DELAYED RELEASE 15 103 71335-2017-7 Duloxetine 180 in 1 BOTTLE CAPSULE, DELAYED RELEASE 180 103 71335-2017-8 Duloxetine 120 in 1 BOTTLE CAPSULE, DELAYED RELEASE 120 103
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71335-2017 DULOXETINE CAPSULE, DELAYED RELEASE [BRYANT RANCH PREPACK] 103 Current NDC, Legacy NDC, 8 package rows 20240809_3fbdcc34-6166-4843-839c-33fed718ffb2.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 9 of 296 · 5,905 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Alcohol Sanitizer Spray. ETHYL ALCOHOL Guangdong Yanze Biotechnology Co., Ltd. 58fb9efe-43f0-1b7f-e063-6394a90a0145 2026-08-14 Warnings Exact identifier unii: 3K9958V90M BM BM63 DROPS CEANOTHUS, KALI ARSEN, KALI MUR, SELENIUM, THALLIUM, WIESBADEN BM Private Limited 59006d82-610a-2e08-e063-6394a90af1ed 2026-08-14 Warnings Exact identifier unii: 059QF0KO0R FRESH FEELS HAND SANITIZER MIST CHILL COCONUT SCENT ETHYL ALCOHOL Amber Glow Cosmetics Limited 6da508ab-176c-4cca-aa1b-c161d9160cd1 2026-08-14 Warnings Exact identifier unii: 3K9958V90M FRESH FEELS HAND SANITIZER MIST ICED CHERRY SCENT ETHYL ALCOHOL Amber Glow Cosmetics Limited eba7108c-7d96-4393-9444-b3ce2ec7a060 2026-08-13 Warnings Exact identifier unii: 3K9958V90M FRESH FEELS HAND SANITIZER MIST BERRY SPRINKLE SCENT ETHYL ALCOHOL Amber Glow Cosmetics Limited 08deb4c2-4ba4-4ec0-b2d2-5cc7f851df4b 2026-08-13 Warnings Exact identifier unii: 3K9958V90M FRESH FEELS HAND SANITIZER MIST BERRY SPRINKLE SWIRL SCENT ETHYL ALCOHOL Amber Glow Cosmetics Limited 424454c9-c1d3-46ec-b186-9159c29f7a4a 2026-08-13 Warnings Exact identifier unii: 3K9958V90M Zep Alcohol Sanitizer ETHANOL Zep Inc. b932a59c-a739-5441-e053-2a95a90a4cfa 2026-08-13 Warnings Exact identifier unii: 3K9958V90M Zep Fuzion Instant Hand Sanitizer ALCOHOL Zep Inc. b43c5701-22ee-1de4-e053-2995a90a8f64 2026-08-13 Warnings Exact identifier unii: 3K9958V90M Zep Instant Hand Sanitizer Gel ALCOHOL Zep Inc. b0ee8023-0128-56d6-e053-2a95a90ab4ed 2026-08-13 Warnings Exact identifier unii: 3K9958V90M Zep Instant Hand Sanitizer Gel ALCOHOL Zep Inc. b0ed98cd-871b-d862-e053-2995a90a14cc 2026-08-13 Warnings Exact identifier unii: 3K9958V90M AFCO 5511 Sanifect E3 ETHANOL Zep Inc. 34795eba-9ec4-6401-e063-6394a90af428 2026-08-13 Warnings Exact identifier unii: 3K9958V90M Alcohol Hand Sanitizer ETHYL ALCOHOL Guangdong Yanze Biotechnology Co., Ltd. 58fa90dc-c3b5-787b-e063-6294a90a2e17 2026-08-13 Warnings Exact identifier unii: 3K9958V90M WISH HAND SANITIZER Mango Coconut Cream ALCOHOL HAND SANITIZER PT SUPER HOME PRODUCT INDONESIA 58faa781-520b-92fa-e063-6294a90a9ecf 2026-08-13 Warnings Exact identifier unii: 3K9958V90M FRESH FEELS HAND SANITIZER MIST COCONUT VANILLA SCENT ETHYL ALCOHOL Amber Glow Cosmetics Limited 89dd227a-365f-4d8b-b21a-4f1c1b5c9c0a 2026-08-13 Warnings Exact identifier unii: 3K9958V90M SprinJene ALCOHOL Health and Natural Beauty USA Corp 1853f023-f4db-4cd8-a4df-a439bc306cc3 2026-08-13 Warnings Exact identifier unii: 3K9958V90M FRESH FEELS HAND SANITIZER MIST WATERMELON POP SCENT ETHYL ALCOHOL Amber Glow Cosmetics Limited 3fea32bb-98ec-4dc6-97d3-c77d8e476c04 2026-08-13 Warnings Exact identifier unii: 3K9958V90M WhiskCare 373 ALCOHOL Whisk Products, Inc. 57d5cd5d-8597-ce66-e063-6394a90a0047 2026-08-12 Warnings Exact identifier unii: 3K9958V90M Zoviro ALCOHOL Zoviro, LLC 9c8ca084-8aef-4616-8d51-aaff3eb25343 2026-08-12 Warnings Exact identifier unii: 3K9958V90M LUXURY IPA 70% LUXURY ISOPROPYL ALCOHOL 70% 16OZ TSM BRANDS LLC 2240a9e0-dac5-54fa-e063-6394a90a35f5 2026-08-11 Warnings Exact identifier unii: ND2M416302 Isopathic Phenolic Rings HOMEOPATHIC LIQUID Energetix Corporation 98a7ca26-ccb7-43c7-bd65-892fcbacc882 2026-08-11 Warnings Exact identifier unii: C151H8M554
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.